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rs794728516

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728516(A;C)
Make rs794728516(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position2583466
GeneKCNQ1
is asnp
is mentioned by
dbSNPrs794728516
ebirs794728516
HLIrs794728516
Exacrs794728516
Varsomers794728516
Maprs794728516
PheGenIrs794728516
hapmaprs794728516
1000 genomesrs794728516
hgdprs794728516
ensemblrs794728516
gopubmedrs794728516
geneviewrs794728516
scholarrs794728516
googlers794728516
pharmgkbrs794728516
gwascentralrs794728516
openSNPrs794728516
23andMers794728516
23andMe allrs794728516
SNP Nexus

SNPshotrs794728516
SNPdbers794728516
MSV3drs794728516
GWAS Ctlgrs794728516
Max Magnitude0
ClinVar
Risk rs794728516(C;C)
Alt rs794728516(C;C)
Reference rs794728516(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNQ1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2604696A>C
CLNSRC
CLNACC RCV000182141.2,